This variation maps to 2 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

LSDB 33032, NP_000286.3:p.THR85MET

HGVS name

None

About this variant

This variant has 2504 individual genotypes and is associated with 3 phenotypes.

Variation displays